Showing results (261-270 of 301) with videos related to
Sort By:
Pageof 31
Proceedings of the National Academy of Sciences of the United States of America|August 3, 2006
Reconstitution of paired T cell receptor alpha- and beta-chains from microdissected single cells of human inflammatory tissuesSabine Seitz, Christian K Schneider, Joachim Malotka, et al.Neurology|March 11, 2014
PREPL deficiency with or without cystinuria causes a novel myasthenic syndromeLuc Régal, Xin-Ming Shen, Duygu Selcen, et al.Annals of Clinical and Translational Neurology|September 28, 2019
Slow-channel myasthenia due to novel mutation in M2 domain of AChR delta subunitXin-Ming Shen, Margherita Milone, Hang-Long Wang, et al.Neuromuscular Disorders : NMD|February 15, 2011
Phenotypic heterogeneity in a large Thai slow-channel congenital myasthenic syndrome kinshipRawiphan Witoonpanich, Teeratorn Pulkes, Charungthai Dejthevaporn, et al.Movement Disorders : Official Journal of the Movement Disorder Society|June 20, 2020
Meta-Analysis of Gut Dysbiosis in Parkinson's DiseaseHiroshi Nishiwaki, Mikako Ito, Tomohiro Ishida, et al.Plos One|February 24, 2009
Ancestral origin of the ATTCT repeat expansion in spinocerebellar ataxia type 10 (SCA10)Teresa Almeida, Isabel Alonso, Sandra Martins, et al.Msystems|December 9, 2020
Short-Chain Fatty Acid-Producing Gut Microbiota Is Decreased in Parkinson's Disease but Not in Rapid-Eye-Movement Sleep Behavior DisorderHiroshi Nishiwaki, Tomonari Hamaguchi, Mikako Ito, et al.Annals of Neurology|July 16, 2008
Dok-7 myasthenia: phenotypic and molecular genetic studies in 16 patientsDuygu Selcen, Margherita Milone, Xin-Ming Shen, et al.Journal of Human Genetics|February 29, 2024
Dyssegmental dysplasia Rolland-Desbuquois type is caused by pathogenic variants in HSPG2 - a founder haplotype shared in five patientsPaniz Farshadyeganeh, Takahiro Yamada, Hirofumi Ohashi, et al.Experimental Neurology|June 7, 2020
A novel fast-channel myasthenia caused by mutation in β subunit of AChR reveals subunit-specific contribution of the intracellular M1-M2 linker to channel gatingXin-Ming Shen, Li Di, Shelley Shen, et al.Pageof 31